Canonical Allele Identifier: CA2082052022

Gene: ALOX5AP

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30745981T>G , CM000675.2:g.30745981T>G	GRCh38
NC_000013.10:g.31320118T>G , CM000675.1:g.31320118T>G	GRCh37
NC_000013.9:g.30218118T>G	NCBI36
NG_011963.2:g.37504T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380490.5:c.170+1822T>G MANE Select	ENSP00000369858.3:n.170+1822T>G
ENST00000380490.4:c.170+1822T>G	ENSP00000369858.3:n.170+1822T>G
ENST00000617770.4:c.341+1822T>G	ENSP00000479870.1:n.341+1822T>G
NM_001204406.1:c.341+1822T>G	NP_001191335.1:n.341+1822T>G
NM_001629.3:c.170+1822T>G	NP_001620.2:n.170+1822T>G
XM_011535024.1:c.*845T>G	XP_011533326.1:n.*845T>G
XM_011535025.1:c.-70-644T>G	XP_011533327.1:n.-70-644T>G
NM_001204406.2:c.341+1822T>G	NP_001191335.1:n.341+1822T>G
NM_001629.4:c.170+1822T>G MANE Select	NP_001620.2:n.170+1822T>G